ephedrine sulfate

Generic: ephedrine sulfate

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name ephedrine sulfate
Generic Name ephedrine sulfate
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

ephedrine sulfate 50 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1325
Product ID 51662-1325_12509d90-9606-7834-e063-6394a90a9a8f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA208943
Listing Expiration 2026-12-31
Marketing Start 2018-10-21

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] adrenergic beta-agonists [moa] increased norepinephrine activity [pe] norepinephrine releasing agent [epc] alpha-adrenergic agonist [epc] beta-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621325
Hyphenated Format 51662-1325

Supplemental Identifiers

RxCUI
1116294
UNII
U6X61U5ZEG

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ephedrine sulfate (source: ndc)
Generic Name ephedrine sulfate (source: ndc)
Application Number NDA208943 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 1 mL in 1 VIAL, SINGLE-DOSE (51662-1325-1)
source: ndc

Packages (1)

51662-1325-1 1 mL in 1 VIAL, SINGLE-DOSE (51662-1325-1)

Ingredients (1)

ephedrine sulfate (50 mg/mL)

Linked Drug Pages (1)

EPHEDRINE SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "12509d90-9606-7834-e063-6394a90a9a8f", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["78c1daef-6e1e-5f2c-e053-2a91aa0a0dba"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (51662-1325-1)", "package_ndc": "51662-1325-1", "marketing_start_date": "20181021"}], "brand_name": "EPHEDRINE SULFATE", "product_id": "51662-1325_12509d90-9606-7834-e063-6394a90a9a8f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Releasing Agent [EPC]", "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "51662-1325", "generic_name": "EPHEDRINE SULFATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EPHEDRINE SULFATE", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "50 mg/mL"}], "application_number": "NDA208943", "marketing_category": "NDA", "marketing_start_date": "20181021", "listing_expiration_date": "20261231"}